Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors for Central Nervous System Metastases from Non-Small Cell Lung Cancer

Oncologist. 2018 Oct;23(10):1199-1209. doi: 10.1634/theoncologist.2017-0572. Epub 2018 Apr 12.

Abstract

Central nervous system (CNS) metastases are a common complication in patients with epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC), resulting in a poor prognosis and limited treatment options. Treatment of CNS metastases requires a multidisciplinary approach, and the optimal treatment options and sequence of therapies are yet to be established. Many systemic therapies have poor efficacy in the CNS due to the challenges of crossing the blood-brain barrier (BBB), creating a major unmet need for the development of agents with good BBB-penetrating biopharmaceutical properties. Although the CNS penetration of first- and second-generation EGFR tyrosine kinase inhibitors (TKIs) is generally low, EGFR-TKI treatment has been shown to delay time to CNS progression in patients with CNS metastases from EGFR-mutated disease. However, a major challenge with EGFR-TKI treatment for patients with NSCLC is the development of acquired resistance, which occurs in most patients treated with a first-line EGFR-TKI. Novel EGFR-TKIs, such as osimertinib, have been specifically designed to address the challenges of acquired resistance and poor BBB permeability and have demonstrated efficacy in the CNS. A rational, iterative drug development process to design agents that could penetrate the BBB could prevent morbidity and mortality associated with CNS disease progression. To ensure a consistent approach to evaluating CNS efficacy, special consideration also needs to be given to clinical trial endpoints.

Implications for practice: Historically, treatment options for patients who develop central nervous system (CNS) metastases have been limited and associated with poor outcomes. The development of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) has improved outcomes for patients with EGFR-mutated disease, and emerging data have demonstrated the ability of these drugs to cross the blood-brain barrier and elicit significant intracranial responses. Recent studies have indicated a role for next-generation EGFR-TKIs, such as osimertinib, in the treatment of CNS metastases. In the context of an evolving treatment paradigm, treatment should be individualized to the patient and requires a multidisciplinary approach.

摘要

在患有表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)患者中,中枢神经系统(CNS)转移是常见的并发症,可致预后不良并且治疗方案有限。CNS转移的治疗需要多学科方法,而最佳的治疗方案和治疗顺序还有待确定。由于存在穿越血脑屏障(BBB)的挑战,许多全身性治疗在CNS中疗效不佳,导致具有良好BBB穿透性生物制药的开发工作,远远未能满足人们的需求。虽然第一代和第二代EGFR酪氨酸激酶抑制剂(TKIs)的CNS渗透率普遍较低,但EGFR‐TKI治疗已显示延缓了EGFR突变的CNS转移患者的CNS进展。然而,获得性耐药是EGFR‐TKI治疗NSCLC患者的一个主要挑战,大多数接受一线EGFR‐TKI治疗的患者都存在这个问题。新的EGFR‐TKI(如Osimertinib)是专门用来解决获得性抗药性和BBB通透性差的难题,并在CNS中显示了疗效。一个可以穿透BBB的合理迭代的药物开发过程,可以防止CNS疾病进展相关的病损率和死亡率。为了确保评估CNS疗效的一致性,还需要特别考虑临床试验终点。

实践意义

一直以来,向出现中枢神经系统(CNS)转移的患者提供的治疗方案很有限,并且与不良预后相关。表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKIs)的发展改善了EGFR突变患者的预后。已经开始有数据显示,这些药物能够跨越血脑屏障,并引起明显的颅内缓解。最近研究表明,新一代EGFR‐TKI(如osimertinib)在治疗CNS转移中起着重要作用。在不断发展的治疗模式中,治疗应针对患者实现个体化,并需要采取多学科方法。

Keywords: Brain metastases; Central nervous system metastases; Epidermal growth factor receptor tyrosine kinase inhibitors; Leptomeningeal metastases; Non‐small cell lung cancer.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Central Nervous System Neoplasms / secondary*
  • ErbB Receptors / antagonists & inhibitors*
  • Humans
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / pathology
  • Neoplasm Metastasis
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use*

Substances

  • Protein Kinase Inhibitors
  • ErbB Receptors